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HRID 344393作成日:2026年10月27日

Benzaldehyde → 4-amino-N-((1-(5-benzylaminopentyl)piperidin-4-yl)methyl)-5-chloro-2-methoxybenzamide

https://huagongshe.com/reaction/344393

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物WaterHCID 962—
反応物Sodium borohydrideHCID 4311764—
反応物4-Amino-N-(1-(5-aminopentyl)piperidin-4-ylmethyl)-5-chloro-2-methoxybenzamideHCID 54008363—
溶媒EthanolHCID 702—
生成物4-amino-N-((1-(5-benzylaminopentyl)piperidin-4-yl)methyl)-5-chloro-2-methoxybenzamideHCID 5401549672%

反応手順

Benzaldehyde (0.76 g) was added to a solution of 4-amino-N-(1-(5-aminopentyl)piperidin-4-ylmethyl)-5-chloro-2-methoxybenzamide (2.0 g) in ethanol (50 ml), and the mixture was stirred at refluxing temperature for 3 hr. Sodium borohydride (0.53 g) was added to the reaction mixture under ice-cooling, and the mixture was stirred overnight at room temperature. Water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, dried and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform:methanol:ammonia=50:5:1) to give 1.78 g of 4-amino-N-((1-(5-benzylaminopentyl)piperidin-4-yl)methyl)-5-chloro-2-methoxybenzamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05864039
出典データセットuspto-grants-1999_01
ORD IDord-d8d6108f1b35472588e42ea8e4f89e05
出典メモuspto-grants-1999_01